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Anthology 71365614Recalls & reported problems

Smith & Nephew, Inc. · ANTHOLOGY BROACH SIZE 14 · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03596010587015), received between Dec 2, 2020 and Dec 2, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Connection Problem” (1 report).

2 other recalls cover devices cleared under the same FDA submission (K123598); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Connection Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryDec 2, 2020Connection Problem; Connection Problem

    IT WAS REPORTED THAT DURING A THR THE DOCTOR HAD EXTREME DIFFICULTY IN EXTRACTING THE BROACH FROM THE FEMUR. HE USED THE STRAIGHT BROACH HANDLE AND HAD TO HIT IT EXTREMELY HARD TO GET BROACH OUT OF FEMUR. PROCEDURE FINISHED WITH COMPETITOR DEVICE. SURGICAL DELAY GREATER THAN 30 MINUTES.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10931774 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K123598. One submission often covers many models, so check the product and lot details in each record.

  • Z-0730-2019 · Jan 7, 2019 · Terminated
    SL PLUS MIA DOUBLE OFFSET ADAPTER RIGHT 60/25MM, S&N 75004613
  • Z-1008-2017 · Nov 16, 2016 · Terminated
    REFLECTION(R) DEAD BLOW MALLET, REF 71362106, QTY: (1), NON-STERILE, Smith & Nephew, Inc,. Memphis, TN 38116

Other Prosthesis, hip, femoral component, cemented, metal devices

All Prosthesis, hip, femoral component, cemented, metal devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.